An ongoing problem: Rhesus hemolytic disease of the newborn - A decade of experience in a single centre

IF 2.3 4区 医学 Q2 PEDIATRICS Pediatrics and Neonatology Pub Date : 2024-09-01 DOI:10.1016/j.pedneo.2024.02.004
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Abstract

Background

The objectives were to evaluate the descriptive features of newborns with a diagnosis of Rhesus (Rh) hemolytic disease, to determine the morbidity and mortality rates, to evaluate the treatment methods and the factors affecting treatment requirements and clinical outcomes during a ten-year period at a tertiary center.

Methods

Newborn infants who had a positive direct Coombs test and/or had a history of intrauterine transfusion (IUT) due to Rh hemolytic disease were included. The data regarding the prenatal, natal and postnatal periods were collected from hospital records.

Results

A total of 260 neonates were included of which 51.2% were female. The mean ± standard deviation gestational age was 36.9 ± 2.7 weeks. The rate of preterm birth was 41.2%. Of 257 mothers whose obstetric medical history could be accessed, 87.2% were multigravida, whereas 76.3% were multiparous. Among mothers who had a reliable history of anti-D immunoglobulin prophylaxis (n=191), 51.3% had not received anti-D immunoglobulin prophylaxis in their previous pregnancies. The antenatal transfusion rate was 31.7% and the frequency of hydrops fetalis was 8.8%. While combined exchange transfusion (ET) and phototherapy (PT) was performed in 15.4% of the babies, the majority either needed phototherapy only (51.1%) or no treatment (33.5%). The mortality rate was 3.8 % (n = 10), and nine babies out of these 10 were those with severe hydrops fetalis.

Conclusion

This study showed that Rh hemolytic disease is still a major problem in developing countries. Multiple comorbidities may occur in addition to life threatening complications, including hydrops fetalis, anemia and severe hyperbilirubinemia. High rates of multiparity and low rates of anti-D immunoglobulin prophylaxis are potential barriers for the eradication of the disease. It should be remembered that Rh hemolytic disease is a preventable disease in the presence of appropriate antenatal follow-up and care facilities.

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一个持续存在的问题:新生儿恒河猴溶血病--一个中心十年的经验。
研究背景目的:评估一家三级医疗中心十年间诊断出Rh溶血病的新生儿的描述性特征,确定发病率和死亡率,评估治疗方法以及影响治疗要求和临床结果的因素:方法:纳入直接库姆斯试验呈阳性和/或因Rh溶血病有宫内输血史(IUT)的新生儿。从医院病历中收集产前、产时和产后的相关数据:结果:共纳入 260 名新生儿,其中 51.2% 为女性。平均胎龄为 36.9±2.7 周。早产率为 41.2%。在 257 名有产科病史的母亲中,87.2%为多胎妊娠,76.3%为多胎妊娠。在有可靠的抗 D 免疫球蛋白预防史的母亲(191 人)中,51.3% 的母亲在之前的妊娠中没有接受过抗 D 免疫球蛋白预防。产前输血率为 31.7%,胎儿水肿发生率为 8.8%。虽然有 15.4% 的婴儿接受了联合交换输血(ET)和光疗(PT),但大多数婴儿只需要光疗(51.1%)或不需要治疗(33.5%)。死亡率为 3.8%(10 人),其中 9 人患有严重的胎儿水肿:本研究表明,Rh 溶血病仍是发展中国家的一个主要问题。除了危及生命的并发症外,还可能出现多种并发症,包括胎儿水肿、贫血和严重的高胆红素血症。多胎妊娠率高和抗 D 免疫球蛋白预防率低是根除这一疾病的潜在障碍。应当记住,如果有适当的产前跟踪和护理设施,Rh 溶血病是一种可以预防的疾病。
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来源期刊
CiteScore
3.10
自引率
0.00%
发文量
170
审稿时长
48 days
期刊介绍: Pediatrics and Neonatology is the official peer-reviewed publication of the Taiwan Pediatric Association and The Society of Neonatology ROC, and is indexed in EMBASE and SCOPUS. Articles on clinical and laboratory research in pediatrics and related fields are eligible for consideration.
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